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The Role of Gene Expression in Embryonic Development

This article explores the basic steps of embryonic development and highlights the importance of gene expression in this process. It discusses the program of differential gene expression, cell differentiation, morphogenesis, and apoptosis. The article also explains the role of cytoplasmic determinants and inductive signals in development.

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The Role of Gene Expression in Embryonic Development

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  1. Objective 7 TSWBatrecognize the basic steps on the embryonic development of organisms and the role that gene expression plays in that development.

  2. Overview: Orchestrating Life’s Processes The development of a fertilized egg into an adult requires a precisely regulated program of gene expression Understanding this program has progressed mainly by studying model organisms Stem cells are key to the developmental process Orchestrating proper gene expression by all cells is crucial for life

  3. Concept 16.1: A program of differential gene expression leads to the different cell types in a multicellular organism A fertilized egg gives rise to many different cell types Cell types are organized successively into tissues, organs, organ systems, and the whole organism Gene expression orchestrates the developmental programs of animals

  4. A Genetic Program for Embryonic Development The transformation from zygote to adult results from cell division, cell differentiation, and morphogenesis

  5. Figure 16.2 1 mm 2 mm (a) Fertilized eggs of a frog (b) Newly hatched tadpole

  6. Figure 16.2a 1 mm (a) Fertilized eggs of a frog

  7. Figure 16.2b 2 mm (b) Newly hatched tadpole

  8. Cell differentiation is the process by which cells become specialized in structure and function The physical processes that give an organism its shape constitute morphogenesis Differential gene expression results from genes being regulated differently in each cell type Materials in the egg can set up gene regulation that is carried out as cells divide

  9. Cytoplasmic Determinants and Inductive Signals An egg’s cytoplasm contains RNA, proteins, and other substances that are distributed unevenly in the unfertilized egg Cytoplasmic determinants are maternal substances in the egg that influence early development As the zygote divides by mitosis, the resulting cells contain different cytoplasmic determinants, which lead to different gene expression

  10. Animation: Cell Signaling Right click slide / Select play

  11. Figure 16.3 (a) Cytoplasmic determinants in the egg (b) Induction by nearby cells Unfertilized egg Early embryo (32 cells) Sperm Nucleus Fertilization Molecules of two different cytoplasmic determinants Zygote (fertilized egg) NUCLEUS Signal transduction pathway Mitotic cell division Signal receptor Two-celled embryo Signaling molecule (inducer)

  12. The other major source of developmental information is the environment around the cell, especially signals from nearby embryonic cells In the process called induction, signal molecules from embryonic cells cause transcriptional changes in nearby target cells Thus, interactions between cells induce differentiation of specialized cell types

  13. Sequential Regulation of Gene Expression During Cellular Differentiation Determination commits a cell irreversibly to its final fate Determination precedes differentiation

  14. Differentiation of Cell Types Today, determination is understood in terms of molecular changes, the expression of genes for tissue-specific proteins The first evidence of differentiation is the production of mRNAs for these proteins Eventually, differentiation is observed as changes in cellular structure

  15. To study muscle cell determination, researchers grew embryonic precursor cells in culture and analyzed them They identified several “master regulatory genes,” the products of which commit the cells to becoming skeletal muscle One such gene is called myoD

  16. Figure 16.4-1 Nucleus Master regulatory gene myoD Other muscle-specific genes DNA Embryonic precursor cell OFF OFF

  17. Figure 16.4-2 Nucleus Master regulatory gene myoD Other muscle-specific genes DNA Embryonic precursor cell OFF OFF mRNA OFF MyoD protein (transcription factor) Myoblast (determined)

  18. Figure 16.4-3 Nucleus Master regulatory gene myoD Other muscle-specific genes DNA Embryonic precursor cell OFF OFF mRNA OFF MyoD protein (transcription factor) Myoblast (determined) mRNA mRNA mRNA mRNA Myosin, other muscle proteins, and cell cycle– blocking proteins MyoD Another transcription factor Part of a muscle fiber (fully differentiated cell)

  19. Apoptosis: A Type of Programmed Cell Death While most cells are differentiating in a developing organism, some are genetically programmed to die Apoptosis is the best-understood type of “programmed cell death” Apoptosis also occurs in the mature organism in cells that are infected, damaged, or at the end of their functional lives

  20. Figure 16.5 2 m

  21. During apoptosis, DNA is broken up and organelles and other cytoplasmic components are fragmented The cell becomes multilobed and its contents are packaged up in vesicles These vesicles are then engulfed by scavenger cells Apoptosis protects neighboring cells from damage by nearby dying cells

  22. Apoptosis is essential to development and maintenance in all animals It is known to occur also in fungi and yeasts In vertebrates, apoptosis is essential for normal nervous system development and morphogenesis of hands and feet (or paws)

  23. Figure 16.6 1 mm Interdigital tissue Cells undergoing apoptosis Space between digits

  24. Figure 16.6a Interdigital tissue 1 mm

  25. Figure 16.6b Cells undergoing apoptosis 1 mm

  26. Figure 16.6c Space between digits 1 mm

  27. Pattern Formation: Setting Up the Body Plan Pattern formation is the development of a spatial organization of tissues and organs In animals, pattern formation begins with the establishment of the major axes Positional information, the molecular cues that control pattern formation, tells a cell its location relative to the body axes and to neighboring cells

  28. Pattern formation has been extensively studied in the fruit fly Drosophila melanogaster Combining anatomical, genetic, and biochemical approaches, researchers have discovered developmental principles common to many other species, including humans

  29. The Life Cycle of Drosophila Fruit flies and other arthropods have a modular structure, composed of an ordered series of segments In Drosophila, cytoplasmic determinants in the unfertilized egg determine the axes before fertilization

  30. Figure 16.7 1 2 3 4 5 Thorax Head Abdomen Follicle cell Egg developing within ovarian follicle Nucleus Egg 0.5 mm Nurse cell Dorsal Right Egg shell Unfertilized egg BODY AXES Posterior Anterior Depleted nurse cells Left Ventral Fertilization Laying of egg (a) Adult Fertilized egg Embryonic development Segmented embryo 0.1 mm Body segments Hatching Larval stage (b) Development from egg to larva

  31. Figure 16.7a Head Thorax Abdomen 0.5 mm Dorsal Right BODY AXES Posterior Anterior Left Ventral (a) Adult

  32. The Drosophila eggs develop in the female’s ovary, surrounded by ovarian cells called nurse cells and follicle cells After fertilization, embryonic development results in a segmented larva, which goes through three stages Eventually the larva forms a cocoon within which it metamorphoses into an adult fly

  33. Figure 16.7b-1 1 Follicle cell Egg developing within ovarian follicle Nucleus Egg Nurse cell (b) Development from egg to larva

  34. Figure 16.7b-2 1 2 Follicle cell Egg developing within ovarian follicle Nucleus Egg Nurse cell Egg shell Unfertilized egg Depleted nurse cells (b) Development from egg to larva

  35. Figure 16.7b-3 1 2 3 Follicle cell Egg developing within ovarian follicle Nucleus Egg Nurse cell Egg shell Unfertilized egg Depleted nurse cells Fertilization Laying of egg Fertilized egg (b) Development from egg to larva

  36. Figure 16.7b-4 1 2 3 4 Follicle cell Egg developing within ovarian follicle Nucleus Egg Nurse cell Egg shell Unfertilized egg Depleted nurse cells Fertilization Laying of egg Fertilized egg Embryonic development Segmented embryo 0.1 mm Body segments (b) Development from egg to larva

  37. Figure 16.7b-5 1 2 3 4 5 Follicle cell Egg developing within ovarian follicle Nucleus Egg Nurse cell Egg shell Unfertilized egg Depleted nurse cells Fertilization Laying of egg Fertilized egg Embryonic development Segmented embryo 0.1 mm Body segments Hatching Larval stage (b) Development from egg to larva

  38. Genetic Analysis of Early Development: Scientific Inquiry Edward B. Lewis, Christiane Nüsslein-Volhard, and Eric Wieschaus won a Nobel Prize in 1995 for decoding pattern formation in Drosophila Lewis discovered the homeotic genes, which control pattern formation in late embryo, larva, and adult stages

  39. Figure 16.8 Wild type Mutant Eye Leg Antenna

  40. Figure 16.8a Wild type Eye Antenna

  41. Figure 16.8b Mutant Leg

  42. Nüsslein-Volhard and Wieschaus studied segment formation They created mutants, conducted breeding experiments, and looked for the corresponding genes Many of the identified mutations were embryonic lethals, causing death during embryogenesis They found 120 genes essential for normal segmentation

  43. Axis Establishment Maternal effect genes encode cytoplasmic determinants that initially establish the axes of the body of Drosophila These maternal effect genes are also called egg-polarity genes because they control orientation of the egg and consequently the fly

  44. One maternal effect gene, the bicoid gene, affects the front half of the body An embryo whose mother has no functional bicoid gene lacks the front half of its body and has duplicate posterior structures at both ends Bicoid: A Morphogen Determining Head Structures

  45. Figure 16.9 Head Tail A8 T2 T1 A7 T3 A6 A5 A1 A2 A4 A3 Wild-type larva 250 m Tail Tail A8 A8 A7 A7 A6 Mutant larva (bicoid)

  46. Figure 16.9a Head Tail A8 T2 T1 A7 T3 A6 A5 A1 A2 A4 A3 Wild-type larva 250 m

  47. Figure 16.9b Tail Tail A8 A8 A7 A7 A6 Mutant larva (bicoid) 250 m

  48. This phenotype suggested that the product of the mother’sbicoid gene is concentrated at the future anterior end and is required for setting up the anterior end of the fly This hypothesis is an example of the morphogen gradient hypothesis; gradients of substances called morphogens establish an embryo’s axes and other features

  49. The bicoid mRNA is highly concentrated at the anterior end of the embryo After the egg is fertilized, the mRNA is translated into Bicoid protein, which diffuses from the anterior end The result is a gradient of Bicoid protein Injection of bicoid mRNA into various regions of an embryo results in the formation of anterior structures at the site of injection

  50. Animation: Head and Tail Axis of a Fruit Fly Right click slide / Select play

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